Excluded / Inactive
NDC Directory Crossover & Product Mapping
The following National Drug Codes (NDCs) are directly associated with the clinical concept for Vardenafil HCl 10 mg Oral Tablet (RxCUI 349479). This crossover tool provides a verified mapping between standardized RxNorm clinical drug definitions and the specific manufactured products listed in the FDA NDC directory.
Healthcare professionals, pharmacists, and data analysts use this list to identify various brand names, labelers, and commercial packaging variations linked to this semantic clinical drug concept. Each entry below represents a commercial product that fulfills the requirements of this specific clinical identifier.
Manufacturer Quick Index
Found 43 manufactured products
APHENA PHARMA SOLUTIONS - TENNESSEE, INC.
NDC Product
Levitra NDC 43353-744
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Levitra NDC 43353-748
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Levitra NDC 67544-507
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Levitra NDC 67544-512
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
Alembic Pharmaceuticals Inc.
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 62332-236
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 62332-237
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 62332-238
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 62332-239
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Limited
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 46708-236
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 46708-237
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 46708-238
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 46708-239
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvKARE
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 42291-847
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 42291-848
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 71335-9696
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 72162-2235
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company, Inc.
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 0527-2800
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 0527-2801
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 0527-2802
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 0527-2803
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Macleods Pharmaceuticals Limited
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 33342-151
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 33342-152
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 33342-153
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 33342-154
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
QYK BRANDS LLC
NDC Product
Vardenafil Hydrochloride NDC 73750-102
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Vardenafil Hydrochloride NDC 73750-103
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Vardenafil Hydrochloride NDC 73750-104
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Vardenafil Hydrochloride NDC 73750-105
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 0093-7652
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 0093-7653
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 0093-7654
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil Hydrochloride NDC 0093-7655
- Generic Name
- Vardenafil Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Lifesciences Limited
NDC Product
Human Prescription DrugVardenafil NDC 70771-1047
- Generic Name
- Vardenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil NDC 70771-1048
- Generic Name
- Vardenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil NDC 70771-1049
- Generic Name
- Vardenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil NDC 70771-1050
- Generic Name
- Vardenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugVardenafil NDC 70710-1068
- Generic Name
- Vardenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil NDC 70710-1069
- Generic Name
- Vardenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil NDC 70710-1070
- Generic Name
- Vardenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVardenafil NDC 70710-1071
- Generic Name
- Vardenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
